ID: ALA3808502

Max Phase: Preclinical

Molecular Formula: C14H9F6N5O2

Molecular Weight: 393.25

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Oc1nc(-c2cc(-c3ccon3)n(CCC(F)(F)C(F)(F)F)n2)ncc1F

Standard InChI:  InChI=1S/C14H9F6N5O2/c15-7-6-21-11(22-12(7)26)9-5-10(8-1-4-27-24-8)25(23-9)3-2-13(16,17)14(18,19)20/h1,4-6H,2-3H2,(H,21,22,26)

Standard InChI Key:  QEYIMKIUNWKNOQ-UHFFFAOYSA-N

Associated Targets(Human)

Liver microsome 8277 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Soluble guanylate cyclase 679 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Liver microsome 4459 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Properties

Molecular Weight: 393.25Molecular Weight (Monoisotopic): 393.0660AlogP: 3.43#Rotatable Bonds: 5
Polar Surface Area: 89.86Molecular Species: NEUTRALHBA: 7HBD: 1
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 10.79CX Basic pKa: CX LogP: 3.85CX LogD: 3.85
Aromatic Rings: 3Heavy Atoms: 27QED Weighted: 0.67Np Likeness Score: -1.23

References

1. Nakai T, Perl NR, Barden TC, Carvalho A, Fretzen A, Germano P, Im GY, Jin H, Kim C, Lee TW, Long K, Moore J, Rohde JM, Sarno R, Segal C, Solberg EO, Tobin J, Zimmer DP, Currie MG..  (2016)  Discovery of IWP-051, a Novel Orally Bioavailable sGC Stimulator with Once-Daily Dosing Potential in Humans.,  (5): [PMID:27190594] [10.1021/acsmedchemlett.5b00479]

Source